Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.2160829A>G	CA123076	INS,INS-IGF2	c.143T>C (p.Phe48Ser) n.202T>C	ClinVar dbSNP
11	g.2160829A>C	CA341285	INS,INS-IGF2	c.143T>G (p.Phe48Cys) n.202T>G	ClinVar dbSNP
11	g.2160829A=	CA1948027016	INS,INS-IGF2	c.143T= (p.Phe48=) n.202T=	dbSNP

Number of alleles fetched